Ning Li

Dr. Ning Li

orcid

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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13 November 2022 in Foods
Verified
Journal Article
Open access
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JTJiao Tan
Jiao Tan
JYJing Yang
Jing Yang
XZXinyi Zhou
Xinyi Zhou
AHAhmed Hamdy
Ahmed Hamdy
XZXilu Zhang
Xilu Zhang
Jiajia SongJiajia Song
Jiajia Song
Inhibition of dipeptidyl peptidase-4 (DPP-4) is an effective way to control blood glucose in diabetic patients. Tenebrio (T.) molitor is an edible insect containing abundant protein. T. molitor protein-derived peptides can suppress the DPP-4 activity. However, the amino acid sequence and binding mechanism of these DPP-4 inhibitory peptides remain unclear. This study used the flavourzyme for T. molitor protein hydrolysis, identified the released peptides with DPP-4 inhibitory effect, and investigated the binding interactions of these peptides with DPP-4. The results showed that flavourzyme efficiently hydrolyzed the T. molitor protein, as demonstrated by the high degree of hydrolysis, disappearance of protein bands in SDS-PAGE, and changes to protein structure. The 4-h flavourzyme hydrolysates showed a good inhibitory effect on DPP-4 (IC50 value of 1.64 mg/mL). The fragment of 1000–3000 Da accounted for 10.39% of the total peptides, but showed the strongest inhibitory effect on DPP-4. The peptides LPDQWDWR and APPDGGFWEWGD were identified from this fraction, and their IC50 values against DPP-4 were 0.15 and 1.03 mg/mL, respectively. Molecular docking showed that these two peptides interacted with the DPP-4 active site via hydrogen bonding, hydrophobic interactions, salt bridge formation, π-cation interactions, and π-π stacking. Our findings indicated that T. molitor protein-derived peptides could be used as natural DPP-4 inhibitors.

1 September 2011 in Carbohydrate Research
Verified
Journal Article
Closed access
NLNing Li
Ning Li
XWXingyue Wei
Xingyue Wei
ZMZheng Mei
Zheng Mei
XXXiaoli Xiong
Xiaoli Xiong
SCShenming Chen
Shenming Chen
SDSheguang Ding
Sheguang Ding

12 February 2010 in Journal of Inclusion Phenomena and Macrocyclic Chemistry
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Journal Article
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NLNing Li
Ning Li
ZMZheng Mei
Zheng Mei
SDSheguang Ding
Sheguang Ding

28 January 2012 in Journal of Inclusion Phenomena and Macrocyclic Chemistry
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Journal Article
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NLNing Li
Ning Li
XLXiao-Mei Lei
Xiao-Mei Lei

1 July 2019 in International Journal of Biological Macromolecules
Verified
Journal Article
Closed access
NLNing Li
Ning Li
XXXiaoli Xiong
Xiaoli Xiong
XHXia Ha
Xia Ha
XWXingyue Wei
Xingyue Wei

14 June 2022 in Catalysts
Verified
Journal Article
Open access
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BXBenjing Xu
Benjing Xu
ZDZiting Du
Ziting Du
JDJinhang Dai
Jinhang Dai
RYRonghe Yang
Ronghe Yang
DYDelong Yang
Delong Yang
FLFukun Li
Fukun Li
Chitin is one of the most abundant biopolymers on Earth but under-utilized. The effective conversion of chitin biomass to useful chemicals is a promising strategy to make full use of chitin. Among chitin-derived compounds, some furan derivatives, typically 5-hydroxymethylfurfural and 3-acetamido-5-acetylfuran, have shown great potential as platform compounds in future industries. In this review, different catalytic systems for the synthesis of nitrogen-free 5-hydroxymethylfurfural and nitrogen-containing 3-acetamido-5-acetylfuran from chitin or its derivatives are summarized comparatively. Some efficient technologies for enhancing chitin biomass conversion have been introduced. Last but not least, future challenges are discussed to enable the production of valuable compounds from chitin biomass via greener processes.